-
1
-
-
77955635233
-
Cancer statistics 2010. CA Cancer
-
Jemal, A., Siegel, R., Xu, J. and Ward, E. (2010) Cancer statistics, 2010. CA Cancer J. Clin., 60, 277-300.
-
(2010)
J. Clin.
, vol.60
, pp. 277-300
-
-
Jemal, A.1
Siegel, R.2
Xu, J.3
Ward, E.4
-
2
-
-
67651089736
-
Concepts in familial colorectal cancer: Where do we stand and what is the future?
-
Castells, A., Castellv́-Bel, S. and Balaguer, F. (2009) Concepts in familial colorectal cancer: where do we stand and what is the future? Gastroenter-ology, 137, 404-409.
-
(2009)
Gastroenter-ology
, vol.137
, pp. 404-409
-
-
Castells, A.1
Castellv́-Bel, S.2
Balaguer, F.3
-
3
-
-
34250887455
-
Review article: Nutrition, obesity and colorectal cancer
-
DOI 10.1111/j.1365-2036.2007.03371.x
-
Johnson, I. T. and Lund, E. K. (2007) Review article: nutrition, obesity and colorectal cancer. Aliment. Pharmacol. Ther., 26, 161-181. (Pubitemid 46985501)
-
(2007)
Alimentary Pharmacology and Therapeutics
, vol.26
, Issue.2
, pp. 161-181
-
-
Johnson, I.T.1
Lund, E.K.2
-
4
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer: Analyses of cohorts of twins from Sweden, Denmark, and Finland
-
DOI 10.1056/NEJM200007133430201
-
Lichtenstein, P., Holm, N. V., Verkasalo, P. K., Iliadou, A., Kaprio, J., Koskenvuo, M., Pukkala, E., Skytthe, A. and Hemminki, K. (2000) Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland. N. Engl. J. Med., 343, 78-85. (Pubitemid 30451850)
-
(2000)
New England Journal of Medicine
, vol.343
, Issue.2
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
Iliadou, A.4
Kaprio, J.5
Koskenvuo, M.6
Pukkala, E.7
Skytthe, A.8
Hemminki, K.9
-
5
-
-
3142733741
-
Familial risk for colorectal cancers are mainly due to heritable causes
-
Hemminki, K. and Chen, B. (2004) Familial risk for colorectal cancers are mainly due to heritable causes. Cancer Epidemiol. Biomarkers Prev., 13, 1253-1256. (Pubitemid 38917917)
-
(2004)
Cancer Epidemiology Biomarkers and Prevention
, vol.13
, Issue.7
, pp. 1253-1256
-
-
Hemminki, K.1
Chen, B.2
-
6
-
-
77951645053
-
Hereditary and familial colon cancer
-
Jasperson, K. W., Tuohy, T. M., Neklason, D. W. and Burt, R. W. (2010) Hereditary and familial colon cancer. Gastroenterology, 138, 2044-2058.
-
(2010)
Gastroenterology
, vol.138
, pp. 2044-2058
-
-
Jasperson, K.W.1
Tuohy, T.M.2
Neklason, D.W.3
Burt, R.W.4
-
7
-
-
20244386256
-
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X
-
DOI 10.1001/jama.293.16.1979
-
Lindor, N. M., Rabe, K., Petersen, G. M. et al. (2005) Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. JAMA, 293, 1979-1985. (Pubitemid 40570891)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1979-1985
-
-
Lindor, N.M.1
Rabe, K.2
Petersen, G.M.3
Haile, R.4
Casey, G.5
Baron, J.6
Gallinger, S.7
Bapat, B.8
Aronson, M.9
Hopper, J.10
Jass, J.11
LeMarchand, L.12
Grove, J.13
Potter, J.14
Newcomb, P.15
Terdiman, J.P.16
Conrad, P.17
Moslein, G.18
Goldberg, R.19
Ziogas, A.20
Anton-Culver, H.21
De Andrade, M.22
Siegmund, K.23
Thibodeau, S.N.24
Boardman, L.A.25
Seminara, D.26
more..
-
8
-
-
67349245787
-
New insights into the aetiology of colorectal cancer from genome-wide association studies
-
Tenesa, A. and Dunlop, M. G. (2009) New insights into the aetiology of colorectal cancer from genome-wide association studies. Nat. Rev. Genet., 10, 353-358.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 353-358
-
-
Tenesa, A.1
Dunlop, M.G.2
-
9
-
-
78049353079
-
Meta-analysis ofthree genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
-
Houlston, R. S., Cheadle, J., Dobbins, S. E. etal. (2010) Meta-analysis ofthree genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat. Genet., 42, 973-977.
-
(2010)
Nat. Genet.
, vol.42
, pp. 973-977
-
-
Houlston, R.S.1
Cheadle, J.2
Dobbins, S.E.3
-
10
-
-
0242363139
-
A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2
-
DOI 10.1073/pnas.2132286100
-
Wiesner, G. L., Daley, D., Lewis, S. et al. (2003) A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2. Proc. Natl Acad. Sci. U S A, 100, 12961-12965. (Pubitemid 37340008)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.22
, pp. 12961-12965
-
-
Wiesner, G.L.1
Daley, D.2
Lewis, S.3
Ticknor, C.4
Platzer, P.5
Lutterbaugh, J.6
MacMillen, M.7
Baliner, B.8
Willis, J.9
Elston, R.C.10
Markowitz, S.D.11
-
11
-
-
33746905921
-
Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1
-
Skoglund, J., Djureinovic, T., Zhou, X. L., Vandrovcova, J., Renkonen, E., Iselius, L., Bisgaard Peltomäki, M. L. P. and Lindblom, A. (2006) Linkage analysis in a large Swedish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 9q22.32-31.1. J. Med. Genet., 43, e7.
-
(2006)
J. Med. Genet.
, vol.43
-
-
Skoglund, J.1
Djureinovic, T.2
Zhou, X.L.3
Vandrovcova, J.4
Renkonen, E.5
Iselius, L.6
Bisgaard Peltomäki, M.L.P.7
Lindblom, A.8
-
12
-
-
33744907495
-
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom
-
DOI 10.1158/0008-5472.CAN-05-4074
-
Kemp, Z. E., Carvajal-Carmona, L. G., Barclay, E. et al. (2006) Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom. Cancer Res., 66, 5003-5006. (Pubitemid 43844919)
-
(2006)
Cancer Research
, vol.66
, Issue.10
, pp. 5003-5006
-
-
Kemp, Z.E.1
Carvajal-Carmona, L.G.2
Barclay, E.3
Gorman, M.4
Martin, L.5
Wood, W.6
Rowan, A.7
Donohue, C.8
Spain, S.9
Jaeger, E.10
Evans, D.G.11
Maher, E.R.12
Bishop, T.13
Thomas, H.14
Houlston, R.15
Tomlinson, I.16
-
13
-
-
77954382262
-
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22
-
Gray-Mc Guire, C., Guda, K., Adrianto, I. et al. (2010) Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. Cancer Res., 70, 5409-5418.
-
(2010)
Cancer Res.
, vol.70
, pp. 5409-5418
-
-
Gray-Mc Guire, C.1
Guda, K.2
Adrianto, I.3
-
14
-
-
33749065163
-
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan
-
DOI 10.1093/hmg/ddl231
-
Kemp, Z., Carvajal-Carmona, L., Spain, S. et al. (2006) Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan. Hum. Mol. Genet., 15, 2903-2910. (Pubitemid 44458121)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.19
, pp. 2903-2910
-
-
Kemp, Z.1
Carvajal-Carmona, L.2
Spain, S.3
Barclay, E.4
Gorman, M.5
Martin, L.6
Jaeger, E.7
Brooks, N.8
Bishop, D.T.9
Thomas, H.10
Tomlinson, I.11
Papaemmanuil, E.12
Webb, E.13
Sellick, G.S.14
Wood, W.15
Evans, G.16
Lucassen, A.17
Maher, E.R.18
Houlston, R.S.19
-
15
-
-
56749180189
-
Deciphering the genetics of hereditary non-syndromic colorectal cancer
-
Papaemmanuil, E., Carvajal-Carmona, L., Sellick, G. S. et al. (2008) Deciphering the genetics of hereditary non-syndromic colorectal cancer. Eur. J. Hum. Genet., 16, 1477-1486.
-
(2008)
Eur. J. Hum. Genet.
, vol.16
, pp. 1477-1486
-
-
Papaemmanuil, E.1
Carvajal-Carmona, L.2
Sellick, G.S.3
-
16
-
-
43549105874
-
Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q
-
Picelli, S., Vandrovcova, J., Jones, S., Djureinovic, T., Skoglund, J., Zhou, X. L., Velculescu, V. E., Vogelstein, B. and Lindblom, A. (2008) Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q. BMC Cancer, 8, 87.
-
(2008)
BMC Cancer
, vol.8
, pp. 87
-
-
Picelli, S.1
Vandrovcova, J.2
Jones, S.3
Djureinovic, T.4
Skoglund, J.5
Zhou, X.L.6
Velculescu, V.E.7
Vogelstein, B.8
Lindblom, A.9
-
17
-
-
77952081574
-
Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer
-
Middeldorp, A., Jagmohan-Changur, S. C., van der Klift, H. M. et al. (2010) Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer. Genes Chromosomes Cancer, 49, 539-548.
-
(2010)
Genes Chromosomes Cancer
, vol.49
, pp. 539-548
-
-
Middeldorp, A.1
Jagmohan-Changur, S.C.2
Van Der Klift, H.M.3
-
18
-
-
69149083658
-
Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancers
-
Guda, K., Moinova, H., He, J. et al. (2009) Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancers. Proc. Natl Acad. Sci. U S A, 106, 12921-12925.
-
(2009)
Proc. Natl Acad. Sci. U S A
, vol.106
, pp. 12921-12925
-
-
Guda, K.1
Moinova, H.2
He, J.3
-
19
-
-
78650465198
-
Evaluation of germline BMP4 mutation as a cause of colorectal cancer
-
Lubbe, S. J., Pittman, A. M., Matijssen, C. et al. (2010) Evaluation of germline BMP4 mutation as a cause of colorectal cancer. Hum. Mutat., 32, E1928-E1938.
-
(2010)
Hum. Mutat.
, vol.32
-
-
Lubbe, S.J.1
Pittman, A.M.2
Et Al., M.3
-
20
-
-
84856869770
-
Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients
-
2010 Dec 2 [Epub ahead ofprint] PMID:21128281
-
Venkatachalam, R., Verwiel, E. T., Kamping, E. J. etal. (2010) Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients. Int. J. Cancer, 2010 Dec 2 [Epub ahead ofprint] PMID:21128281.
-
(2010)
Int. J. Cancer
-
-
Venkatachalam, R.1
Verwiel, E.T.2
Kamping, E.J.3
-
21
-
-
3843123047
-
Frequency of hereditary non-polyposis colorectal cancer and other colorectal cancer familial forms in Spain: A multicentre, prospective, nationwide study
-
DOI 10.1097/00042737-200401000-00007
-
Piñol, V., Andreu, M., Castells, A., Payá, A., Bessa, X., Rodrigo, J. and Gastrointestinal Oncology Group of the Spanish Gastroenterological Association (2004) Frequency of hereditary non-polyposis colorectal cancer and other colorectal cancer familial forms in Spain: a multicentre, prospective, nationwide study. Eur. J. Gastroenterol. Hepatol., 16, 39-45. (Pubitemid 39043701)
-
(2004)
European Journal of Gastroenterology and Hepatology
, vol.16
, Issue.1
, pp. 39-45
-
-
Pinol, V.1
Andreu, M.2
Castells, A.3
Paya, A.4
Bessa, X.5
Jover, R.6
-
22
-
-
3042704106
-
Synchronous colorectal neoplasms in patients with colorectal cancer: Predisposing individual and familial factors
-
Piñol, V., Andreu, M., Castells, A., Payá, A., Bessa, X., Jover, R., Gastrointestinal Oncology Group of the Spanish Gastroenterological Association et al. (2004) Synchronous colorectal neoplasms in patients with colorectal cancer: predisposing individual and familial factors. Dis. Colon. Rectum, 47, 1192-1200. (Pubitemid 38857072)
-
(2004)
Diseases of the Colon and Rectum
, vol.47
, Issue.7
, pp. 1192-1200
-
-
Pinol, V.1
Andreu, M.2
Castells, A.3
Paya, A.4
Bessa, X.5
Jover, R.6
-
23
-
-
27144484911
-
Differential features of colorectal cancers fulfilling Amsterdam criteria without involvement of the mutator pathway
-
DOI 10.1158/1078-0432.CCR-05-0965
-
Llor, X., Pons, E., Xicola, R. M. et al. (2005) Differential features of colorectal cancers fulfilling Amsterdam criteria without involvement of the mutator pathway. Clin. Cancer Res., 11, 7304-7310. (Pubitemid 41507688)
-
(2005)
Clinical Cancer Research
, vol.11
, Issue.20
, pp. 7304-7310
-
-
Llor, X.1
Pons, E.2
Xicola, R.M.3
Castells, A.4
Alenda, C.5
Pinol, V.6
Andreu, M.7
Castellvi-Bel, S.8
Paya, A.9
Jover, R.10
Bessa, X.11
Giros, A.12
Roca, A.13
Gassull, M.A.14
-
24
-
-
34447108769
-
Detection of metachronous neoplasms in colorectal cancer patients: Identification of risk factors
-
DOI 10.1007/s10350-007-0237-2
-
Ballesté, B., Bessa, X., Piñol, V. et al. (2007) Detection of metachronous neoplasms in colorectal cancer patients: identification of risk factors. Dis. Colon. Rectum, 50, 971-980. (Pubitemid 47030192)
-
(2007)
Diseases of the Colon and Rectum
, vol.50
, Issue.7
, pp. 971-980
-
-
Balleste, B.1
Bessa, X.2
Pinol, V.3
Castellvi-Bel, S.4
Castells, A.5
Alenda, C.6
Paya, A.7
Jover, R.8
Xicola, R.M.9
Pons, E.10
Llor, X.11
Cordero, C.12
Fernandez-Banares, F.13
De Castro, L.14
Rene, J.M.15
Andreu, M.16
-
25
-
-
20244386395
-
Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer
-
DOI 10.1001/jama.293.16.1986
-
Piñol, V., Castells, A., Andreu, M. et al. (2005) Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer. JAMA, 293, 1986-1994 (Pubitemid 40570892)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1986-1994
-
-
Pinol, V.1
Castells, A.2
Andreu, M.3
Castellvi-Bel, S.4
Alenda, C.5
Llor, X.6
Xicola, R.M.7
Rodriguez-Moranta, F.8
Paya, A.9
Jover, R.10
Bessa, X.11
-
26
-
-
21144444336
-
Genomic rearrangements in MSH2 and MLH1 are rare mutational events in Spanish patients with hereditary nonpolyposis colorectal cancer
-
DOI 10.1016/j.canlet.2005.01.036, PII S0304383505001059
-
Castellv́-Bel, S., Castells, A., Strunk, M. et al. (2005) Genomic rearrange-ments in MSH2 and MLH1 are rare mutational events in Spanish patients with hereditary nonpolyposis colorectal cancer. Cancer Lett., 225, 93-98. (Pubitemid 40732772)
-
(2005)
Cancer Letters
, vol.225
, Issue.1
, pp. 93-98
-
-
Castellvi-Bel, S.1
Castells, A.2
Strunk, M.3
Ferrandez, A.4
Piazuelo, E.5
Mila, M.6
Pinol, V.7
Rodriguez-Moranta, F.8
Andreu, M.9
Lanas, A.10
Pique, J.M.11
-
27
-
-
70449526177
-
Association of MUTYH and MSH6 germline mutations in colorectal cancer patients
-
Giráldez, M. D., Balaguer, F., Caldés, T. et al. (2009) Association of MUTYH and MSH6 germline mutations in colorectal cancer patients. Fam. Cancer, 8, 525-531.
-
(2009)
Fam. Cancer
, vol.8
, pp. 525-531
-
-
Giráldez, M.D.1
Balaguer, F.2
Caldés, T.3
-
28
-
-
33947280508
-
Identification of MYH Mutation Carriers in Colorectal Cancer: A Multicenter, Case-Control, Population-Based Study
-
DOI 10.1016/j.cgh.2006.12.025, PII S1542356506013231
-
Balaguer, F., Castellv́-Bel, S., Castells, A. et al. (2007) Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study. Clin. Gastroenterol. Hepatol., 5, 379-387. (Pubitemid 46420561)
-
(2007)
Clinical Gastroenterology and Hepatology
, vol.5
, Issue.3
, pp. 379-387
-
-
Balaguer, F.1
Castellvi-Bel, S.2
Castells, A.3
Andreu, M.4
Munoz, J.5
Gisbert, J.P.6
Llor, X.7
Jover, R.8
De Cid, R.9
Gonzalo, V.10
Bessa, X.11
Xicola, R.M.12
Pons, E.13
Alenda, C.14
Paya, A.15
Pique, J.M.16
-
29
-
-
33645691923
-
Cyclooxygenase 2 expression in colorectal cancer with DNA mismatch repair deficiency
-
Castells, A., Payá, A., Alenda, C. et al. (2006) Cyclooxygenase 2 expression in colorectal cancer with DNA mismatch repair deficiency. Clin. Cancer Res., 12, 1686-1692.
-
(2006)
Clin. Cancer Res.
, vol.12
, pp. 1686-1692
-
-
Castells, A.1
Payá, A.2
Alenda, C.3
-
30
-
-
33847712926
-
Performance of different microsatellite marker panels for detection of mismatch repair-deficient colorectal tumors
-
Xicola, R. M., Llor, X., Pons, E. et al. (2007) Performance of different microsatellite marker panels for detection of mismatch repair-deficient colorectal tumors. J. Natl Cancer Inst., 99, 244-252.
-
(2007)
J. Natl Cancer Inst.
, vol.99
, pp. 244-252
-
-
Xicola, R.M.1
Llor, X.2
Pons, E.3
-
31
-
-
38749113701
-
A prospective, multicenter, population-based study of BRAF mutational analysis for Lynch syndrome screening
-
Bessa, X., Ballesté, B., Andreu, M. etal. (2008) A prospective, multicenter, population-based study of BRAF mutational analysis for Lynch syndrome screening. Clin. Gastroenterol. Hepatol., 6, 206-214.
-
(2008)
Clin. Gastroenterol. Hepatol.
, vol.6
, pp. 206-214
-
-
Bessa, X.1
Ballesté, B.2
Et Al., A.M.3
-
32
-
-
77649288717
-
Aberrant gene promoter methylation associated with sporadic multiple colorectal cancer
-
Gonzalo, V., Lozano, J. J., Muñoz, J. et al. (2010) Aberrant gene promoter methylation associated with sporadic multiple colorectal cancer. PLo S One, 5, e8777
-
(2010)
PLo S One
, vol.5
-
-
Gonzalo, V.1
Lozano, J.J.2
Muñoz, J.3
-
33
-
-
33646560325
-
Clinical performance of original and revised Bethesda guidelines for the identification of MSH2/MLH1 gene carriers in patients with newly diagnosed colorectal cancer: Proposal of a new and simpler set of recommendations
-
DOI 10.1111/j.1572-0241.2006.00522.x
-
Rodŕguez-Moranta, F., Castells, A., Andreu, M. et al. (2006) Clinical performance of original and revised Bethesda guidelines for the identification of MSH2/MLH1 gene carriers in patients with newly diagnosed colorectal cancer: proposal of a new and simpler set of recommendations. Am. J. Gastroenterol., 101, 1104-1111. (Pubitemid 43725327)
-
(2006)
American Journal of Gastroenterology
, vol.101
, Issue.5
, pp. 1104-1111
-
-
Rodriguez-Moranta, F.1
Castells, A.2
Andreu, M.3
Pinol, V.4
Castellvi-Bel, S.5
Alenda, C.6
Llor, X.7
Xicola, R.M.8
Jover, R.9
Paya, A.10
Bessa, X.11
Balaguer, F.12
Cubiella, J.13
Arguello, L.14
Morillas, J.D.15
Bujanda, L.16
-
34
-
-
37449019456
-
Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients
-
Balaguer, F. Balmaña, J. Castellv́-Bel, S. et al. (2008) Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients. Gastroenterology, 134, 39-46.
-
(2008)
Gastroenterology
, vol.134
, pp. 39-46
-
-
Balaguer, F.1
Balmaña, J.2
Castellv́-Bel, S.3
-
35
-
-
51849147419
-
Comparison of predictive models, clinical criteria and molecular tumour screening for the identification ofpatients with Lynch syndrome in a population-based cohort of colorectal cancer patients
-
Balmaña, J., Balaguer, F., Castellv́-Bel, S. et al. (2008) Comparison of predictive models, clinical criteria and molecular tumour screening for the identification ofpatients with Lynch syndrome in a population-based cohort of colorectal cancer patients. J. Med. Genet., 45, 557-563.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 557-563
-
-
Balmaña, J.1
Balaguer, F.2
Castellv́-Bel, S.3
-
36
-
-
33646798052
-
Mismatch repair status in the prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer
-
DOI 10.1136/gut.2005.073015
-
Jover, R., Zapater, P., Castells, A. et al. (2006) Mismatch repair status in the prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer. Gut, 55, 848-855. (Pubitemid 43764557)
-
(2006)
Gut
, vol.55
, Issue.6
, pp. 848-855
-
-
Jover, R.1
Zapater, P.2
Castells, A.3
Llor, X.4
Andreu, M.5
Cubiella, J.6
Pinol, V.7
Xicola, R.M.8
Bujanda, L.9
Rene, J.M.10
Clofent, J.11
Bessa, X.12
Morillas, J.D.13
Nicolas-Perez, D.14
Paya, A.15
Alenda, C.16
-
37
-
-
59249097606
-
The efficacy of adjuvant chemotherapy with 5-fluorouracil in colorectal cancer depends on the mismatch repair status
-
Jover, R., Zapater, P., Castells, A. et al. (2009) The efficacy of adjuvant chemotherapy with 5-fluorouracil in colorectal cancer depends on the mismatch repair status. Eur. J. Cancer, 45, 365-373
-
(2009)
Eur. J. Cancer
, vol.45
, pp. 365-373
-
-
Jover, R.1
Zapater, P.2
Castells, A.3
-
38
-
-
34548088316
-
Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer
-
DOI 10.1093/carcin/bgm098
-
Castellv́-Bel, S., Castells, A., de Cid, R. et al. (2007) Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer. Carcinogenesis, 28, 1687-1691. (Pubitemid 47289029)
-
(2007)
Carcinogenesis
, vol.28
, Issue.8
, pp. 1687-1691
-
-
Castellvi-Bel, S.1
Castells, A.2
De Cid, R.3
Munoz, J.4
Balaguer, F.5
Gonzalo, V.6
Ruiz-Ponte, C.7
Andreu, M.8
Llor, X.9
Jover, R.10
Bessa, X.11
Xicola, R.M.12
Pons, E.13
Alenda, C.14
Paya, A.15
Carracedo, A.16
Pique, J.M.17
-
39
-
-
76149083554
-
Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: A two-stage case-control study
-
Fernández-Rozadilla, C., Tarŕo, R., Clofent, J. et al. (2010) Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: a two-stage case-control study. Cancer Epidemiol. Biomarkers Prev., 19, 619-623.
-
(2010)
Cancer Epidemiol. Biomarkers Prev.
, vol.19
, pp. 619-623
-
-
Fernández-Rozadilla, C.1
Tarŕo, R.2
Clofent, J.3
-
40
-
-
77958531223
-
Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohort
-
Fernández-Rozadilla, C., de Castro, L., Clofent, J. et al. (2010) Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohort. PLo S One, 5, e12673.
-
(2010)
PLo S One
, vol.5
-
-
Fernández-Rozadilla, C.1
De Castro, L.2
Clofent, J.3
-
41
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
DOI 10.1038/ng.111, PII NG111
-
Tomlinson, I. P., Webb, E., Carvajal-Carmona, L. et al. (2008) A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat. Genet., 40, 623-630. (Pubitemid 351601204)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 623-630
-
-
Tomlinson, I.P.M.1
Webb, E.2
Carvajal-Carmona, L.3
Broderick, P.4
Howarth, K.5
Pittman, A.M.6
Spain, S.7
Lubbe, S.8
Walther, A.9
Sullivan, K.10
Jaeger, E.11
Fielding, S.12
Rowan, A.13
Vijayakrishnan, J.14
Domingo, E.15
Chandler, I.16
Kemp, Z.17
Qureshi, M.18
Farrington, S.M.19
Tenesa, A.20
Prendergast, J.G.D.21
Barnetson, R.A.22
Penegar, S.23
Barclay, E.24
Wood, W.25
Martin, L.26
Gorman, M.27
Thomas, H.28
Peto, J.29
Bishop, D.T.30
Gray, R.31
Maher, E.R.32
Lucassen, A.33
Kerr, D.34
Evans, D.G.R.35
Schafmayer, C.36
Buch, S.37
Volzke, H.38
Hampe, J.39
Schreiber, S.40
John, U.41
Koessler, T.42
Pharoah, P.43
Van Wezel, T.44
Morreau, H.45
Wijnen, J.T.46
Hopper, J.L.47
Southey, M.C.48
Giles, G.G.49
Severi, G.50
Castellvi-Bel, S.51
Ruiz-Ponte, C.52
Carracedo, A.53
Castells, A.54
Forsti, A.55
Hemminki, K.56
Vodicka, P.57
Naccarati, A.58
Lipton, L.59
Ho, J.W.C.60
Cheng, K.K.61
Sham, P.C.62
Luk, J.63
Agundez, J.A.G.64
Ladero, J.M.65
De La Hoya, M.66
Caldes, T.67
Niittymaki, I.68
Tuupanen, S.69
Karhu, A.70
Aaltonen, L.71
Cazier, J.-B.72
Campbell, H.73
Dunlop, M.G.74
Houlston, R.S.75
more..
-
42
-
-
56049119387
-
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer
-
Pittman, A. M., Webb, E., Carvajal-Carmona, L. et al. (2008) Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. Hum. Mol. Genet., 17, 3720-3727
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3720-3727
-
-
Pittman, A.M.1
Webb, E.2
Carvajal-Carmona, L.3
-
43
-
-
77956134067
-
Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype
-
Abuĺ, A., Bessa, X., González, J. R. et al. (2010) Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype. Gastroenterology, 139, 788-796.
-
(2010)
Gastroenterology
, vol.139
, pp. 788-796
-
-
Abuĺ, A.1
-
44
-
-
75549083862
-
COGENT (COlorectal cancer GENe Tics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer
-
Tomlinson, I. P., Dunlop, M., Campbell, H. et al. (2010) COGENT (COlorectal cancer GENe Tics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. Br. J. Cancer, 102, 447-454.
-
(2010)
Br. J. Cancer
, vol.102
, pp. 447-454
-
-
Tomlinson, I.P.1
Dunlop, M.2
Campbell, H.3
-
45
-
-
72849144434
-
Sequencing technologies - The next generation
-
Metzker, M. L. (2010) Sequencing technologies - the next generation. Nat. Rev. Genet., 11, 31-46.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
46
-
-
77951115122
-
International network of cancer genome projects
-
International Cancer Genome Consortium
-
International Cancer Genome Consortium, Hudson, T. J., Anderson, W. et al. (2010) International network of cancer genome projects. Nature, 464, 993-998
-
(2010)
Nature
, vol.464
, pp. 993-998
-
-
Hudson, T.J.1
Anderson, W.2
-
47
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium
-
1000 Genomes Project Consortium, Durbin, R. M., Abecasis, G. R. et al. (2010) A map of human genome variation from population-scale sequencing. Nature, 467, 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Durbin, R.M.1
Abecasis, G.R.2
-
48
-
-
77449121614
-
Target-enrichment strategies for next-generation sequencing
-
Mamanova, L., Coffey, A. J., Scott, C. E., Kozarewa, I., Turner, E. H., Kumar, A., Howard, E., Shendure, J. and Turner, D. J. (2010) Target-enrichment strategies for next-generation sequencing. Nat Methods, 7, 111-118.
-
(2010)
Nat Methods
, vol.7
, pp. 111-118
-
-
Mamanova, L.1
Coffey, A.J.2
Scott, C.E.3
Kozarewa, I.4
Turner, E.H.5
Kumar, A.6
Howard, E.7
Shendure, J.8
Turner, D.J.9
-
49
-
-
70249111091
-
Targeted capture and massively parallel sequencing of 12 human exomes
-
Ng, S. B., Turner, E. H., Robertson, P. D. et al. (2009) Targeted capture and massively parallel sequencing of 12 human exomes. Nature, 461, 272-276.
-
(2009)
Nature
, vol.461
, pp. 272-276
-
-
Ng, S.B.1
Turner, E.H.2
Robertson, P.D.3
-
50
-
-
79952198057
-
Exome sequencing: The sweet spot before whole genomes
-
Teer, J. K. and Mullikin, J. C. (2010) Exome sequencing: the sweet spot before whole genomes. Hum. Mol. Genet., 19, R145-R151.
-
(2010)
Hum. Mol. Genet.
, vol.19
-
-
Teer, J.K.1
Mullikin, J.C.2
|